Foxd2 Dysfunction is Implicated in Syndromic Congenital Anomalies of the Kidney and Urinary Tract (cakut)

FOXD2 Res Consortium

Foxd2 Dysfunction is Implicated in Syndromic Congenital Anomalies of the Kidney and Urinary Tract (cakut)

FOXD2 Res Consortium

Araştırma sonucu: Dergiye katkı › Toplantı Özeti › bilirkişi

Orijinal dil	İngilizce
Sayfa (başlangıç-bitiş)	S128-S129
Sayfa sayısı	2
Dergi	Pediatric Nephrology
Hacim	38
Yayın durumu	Yayınlandı - Eyl 2023

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@article{d613337c4f5d4c60a6b1408bae6535d2,

title = "Foxd2 Dysfunction is Implicated in Syndromic Congenital Anomalies of the Kidney and Urinary Tract (cakut)",

author = "\{FOXD2 Res Consortium\} and Korbinian Riedhammer and Thanh-Minh Nguyen and Can Kosukcu and Julia Calzada-Wack and Yong Li and Seha Saygili and Gwang-Jin Kim and Salim Caliskan and Anna Koettgen and Sebastian Arnold and Fatih Ozaltin and Miriam Schmidts and Julia Hoefele",

year = "2023",

month = sep,

language = "English",

volume = "38",

pages = "S128--S129",

journal = "Pediatric Nephrology",

issn = "0931-041X",

publisher = "Springer Science and Business Media Deutschland GmbH",

}

TY - JOUR

T1 - Foxd2 Dysfunction is Implicated in Syndromic Congenital Anomalies of the Kidney and Urinary Tract (cakut)

AU - FOXD2 Res Consortium

AU - Riedhammer, Korbinian

AU - Nguyen, Thanh-Minh

AU - Kosukcu, Can

AU - Calzada-Wack, Julia

AU - Li, Yong

AU - Saygili, Seha

AU - Kim, Gwang-Jin

AU - Caliskan, Salim

AU - Koettgen, Anna

AU - Arnold, Sebastian

AU - Ozaltin, Fatih

AU - Schmidts, Miriam

AU - Hoefele, Julia

PY - 2023/9

Y1 - 2023/9

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:001091418900181&DestLinkType=FullRecord&DestApp=WOS_CPL

M3 - Meeting Abstract

SN - 0931-041X

VL - 38

SP - S128-S129

JO - Pediatric Nephrology

JF - Pediatric Nephrology

ER -